Canonical Allele Identifier: CA2782024499

Gene: ZHX2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.122960820G>A , CM000670.2:g.122960820G>A	GRCh38
NC_000008.10:g.123973060G>A , CM000670.1:g.123973060G>A	GRCh37
NC_000008.9:g.124042241G>A	NCBI36
NG_046951.1:g.184472G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000314393.6:c.*4+6792G>A MANE Select	ENSP00000314709.4:n.*4+6792G>A
ENST00000314393.5:c.*4+6792G>A	ENSP00000314709.4:n.*4+6792G>A
NM_014943.3:c.*4+6792G>A	NP_055758.1:n.*4+6792G>A
XM_005250836.3:c.*4+6792G>A	XP_005250893.1:n.*4+6792G>A
XM_005250837.3:c.*4+6792G>A	XP_005250894.1:n.*4+6792G>A
XM_011516931.1:c.*4+6792G>A	XP_011515233.1:n.*4+6792G>A
XM_011516932.1:c.*4+6792G>A	XP_011515234.1:n.*4+6792G>A
NM_001362797.1:c.*4+6792G>A	NP_001349726.1:n.*4+6792G>A
NM_014943.4:c.*4+6792G>A	NP_055758.1:n.*4+6792G>A
XM_005250836.5:c.*4+6792G>A	XP_005250893.1:n.*4+6792G>A
XM_011516932.3:c.*4+6792G>A	XP_011515234.1:n.*4+6792G>A
NM_014943.5:c.*4+6792G>A MANE Select	NP_055758.1:n.*4+6792G>A
NM_001362797.2:c.*4+6792G>A	NP_001349726.1:n.*4+6792G>A